Microtubule Tracking in Electron Microscopy Volumes
We present a method for microtubule tracking in electron microscopy volumes. Our method first identifies a sparse set of voxels that likely belong to microtubules. Similar to prior work, we then enumerate potential edges between these voxels, which we represent in a candidate graph. Tracks of microt...
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Main Authors: | , , , |
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Format: | Journal Article |
Language: | English |
Published: |
17-09-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | We present a method for microtubule tracking in electron microscopy volumes.
Our method first identifies a sparse set of voxels that likely belong to
microtubules. Similar to prior work, we then enumerate potential edges between
these voxels, which we represent in a candidate graph. Tracks of microtubules
are found by selecting nodes and edges in the candidate graph by solving a
constrained optimization problem incorporating biological priors on microtubule
structure. For this, we present a novel integer linear programming formulation,
which results in speed-ups of three orders of magnitude and an increase of 53%
in accuracy compared to prior art (evaluated on three 1.2 x 4 x 4$\mu$m volumes
of Drosophila neural tissue). We also propose a scheme to solve the
optimization problem in a block-wise fashion, which allows distributed tracking
and is necessary to process very large electron microscopy volumes. Finally, we
release a benchmark dataset for microtubule tracking, here used for training,
testing and validation, consisting of eight 30 x 1000 x 1000 voxel blocks (1.2
x 4 x 4$\mu$m) of densely annotated microtubules in the CREMI data set
(https://github.com/nilsec/micron). |
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DOI: | 10.48550/arxiv.2009.08371 |